Teleflex Medical recalls Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E2

Recalled April 30, 2014 · FDA recall Z-1497-2014 · Teleflex Medical

Hazard

The products are being recalled because they did not meet minimum diameter requirements. · FDA Class II

Units

3,816 ea

Sold at

Worldwide Distribution - CA, CO, FL, IN, KY, MA, NM, PA, Canada, Ireland and Germany.

Description

The products are being recalled because they did not meet minimum diameter requirements.

Product

Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.

Manufacturer(s)

Teleflex Medical

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →